Anim. Syst. Evol. Divers. Vol. 37, No. 3: 242-248, July 2021 https://doi.org/10.5635/ASED.2021.37.3.016

Short communication Lobohalacarus weberi (, Halacaridae) from Shallow Ground Waters in South Korea

Jong Hak Shin1, Jimin Lee2, Cheon Young Chang1,*

1Department of Biological Science, Daegu University, Gyeongsan 38453, Korea 2Marine Ecosystem Research Center, Korea Institute of Ocean Science & Technology, Busan 49111, Korea

ABSTRACT

Lobohalacarus weberi (Romijn and Viets, 1924) is added to the halacarid fauna of Korea as the third member of freshwater halacarid species. Both the genus and species are newly recorded from Korea. Halacarid mites were collected from two hillside wells and a streamside hyporheic zone in the southeastern region of South Korea. Lobohalacarus weberi is characterized by a well-developed frontal spine-like process, seven dorsal setae, the fourth segment of palp with a short distal and three long proximal setae, and tibiae of legs II to IV with two, one, two pectinate setae, respectively. A few minor individual variabilities were observed in the number of perigenital seta and genital acetabula, the setal armature on genua of legs, and the shape of spinule row on lateral claws. Keywords: ‌description, freshwater, halacarid mite, hyporheic zone, new record, wells

INTRODUCTION Voucher specimens are kept in the specimen room of the Department of Biological Science, Daegu University (DB), As shown in the taxon name of “Halacarida” (meaning ‘aca­ Gyeongsan, Korea. rids from salt waters’), halacarids are basically marine. Terminology and abbreviations in the text and figure cap­ Only 67 species or subspecies of 17 genera (about 6% of tions follow Bartsch (2006): AD, anterior dorsal plate; AE, the total number of species currently recorded in the family anterior epimeral plate; ds, dorsal setae on idiosoma (ds- Halacaridae Murray, 1877) are freshwater or brackish-water 2, second dorsal setae on idiosoma); GA, genitoanal plate; (Bartsch, 2018; FADA, 2021). Recently, we have collected gac, genital acetabula; glp, gland pore(s), numbered glp-1 to four halacarid mites at two hillside wells and a streamside hy­ glp-5 from anterior to posterior; GO, genital opening; OC, porheic zone in the southeastern region of South Korea (Fig. ocular plate(s); P, palp (P-2, second palpal segment); pas, 1). They are identified as the Lobohalacarus weberi (Romijn parambulacral setae; PD, posterior dorsal plate; PE, poste­ and Viets, 1924), notwithstanding a few minor morphological rior epimeral plate; pgs, perigenital setae; sgs, subgenital variations were observed among the specimens examined. setae. Herein we redescribe it as a new record from South Korea. Following the two former records, Soldanellonyx chappui- SYSTEMATIC ACOOUNTS si Walter, 1917 by Imamura (1968) and S. monardi Walter, 1919 by Shin and Chang (2021), this is the third report on the Subclass Acari Leach, 1817 freshwater halacarid mites from Korea. Order Reuter, 1909 Methods for field and laboratory works, such as collec­ Suborder Prostigmata Kramer, 1877 tion, preparation for microscope examination, drawings and Superfamily Halacaroidea Murray, 1877 measurements, are the same as in our previous studies (Lee Family Halacaridae Murray, 1877 and Chang, 2017; Shin and Chang, 2019, 2021). 1*Genus Lobohalacarus Viets, 1939

Korean name: 1*거북등짠물응애속 (신칭)

This is an Open Access article distributed under the terms of the Creative *To whom correspondence should be addressed Commons Attribution Non-Commercial License (http://creativecommons.org/ Tel: 82-53-850-6454, Fax: 82-53-850-6459 licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, E-mail: [email protected] and reproduction in any medium, provided the original work is properly cited. eISSN 2234-8190 Copyright The Korean Society of Systematic Zoology Lobohalacarus weberi (Halacaridae), New Record from Korea

Fig. 1. Localities. A, A map showing three collection sites in South Korea: 1, Gyeongsan; 2, Pohang; 3, Ulsan; B, A well in Gyeong- san; C, A well in Pohang; D, Jujeon valley, Ulsan.

1*Lobohalacarus weberi (Romijn and Viets, 1924) ae irregularly. AD 94 μm long, 68 μm wide (length to width (Figs. 2, 3) ratio about 1.38); anterior part blunt triangular-shaped, pos­ Walterella weberi Romijn and Viets, 1924: 217, figs. -3 6; terior margin nearly straight or slightly concave, and the Walter and Bader, 1952: 224, fig. 58. widest at level of 3/4 of AD. OC elongated and narrowing Lobohalacarus weberi: Viets, 1939: 506; Green and Mac­ posteriorly, 62 μm long, 23 μm wide (length to width ratio Quitty, 1987: 162, fig. 68A-D; Bartsch, 2006: 128, fig. about 2.70); corneae and glp absent. PD large, 1.91 times 5-8a-f; 2011: 493, fig. 3A-C; 2018: 85, fig. 4A-E. longer than wide, 157 μm long, 82 μm wide; anterior margin Walterella weberi quadripora Walter, 1947: 236, fig. 35 (cit­ wider than posterior one and both margin nearly straight or ed from Bartsch, 2018). slightly arched. Seven pairs of dorsal setae (ds) short: ds-1 Lobohalacarus weberi quadriporus: Bartsch, 1975: 35, figs. located between frontal process and anterior AD; ds-2 situ­ 38-53. ated near anterior margin of 1/3 AD; ds-3 and ds-4 located on OC, ds-3 at anterolateral corner of OC and ds-4 at half of Material examined. Korea: 1♀ (DB50040), Gyeongsang­ OC; remaining 3 dorsal setae (ds-5-7) evenly spaced 1/3 of buk-do: Gyeongsan-si, Sajeong-dong, a well (near Gyeong­ PD, from anterior third PD to posterior margin of PD. san railway station), 33°43ʹ16ʺN, 128°43ʹ39ʺ, 31 Mar 2020, All ventral plates (AE, PE, and GA) fused (Fig. 2B) and Chang CY; 1♀ (DB50041), Pohang-si, Donghae-myeon, ornamented with numerous foveae. The region correspond­ Heunghwan-ri, a well (in a seaside village), 36°01ʹ43ʺN, ing AE with 3 pairs of ventral setae, and pair of epimeral 129°30ʹ14ʺE, 23 Jul 2020, Chang CY and Shin JH; 1♀ pores present near trochanter of leg II. PE region with 1 (DB50042), same locality as previous, 9 Oct 2020, Shin JH; short dorsal, 1 long lateral and 1 ventral seta. GO (Fig. 2B, 1♀ (DB50043), Ulsan-si, Jujeon-dong, Jujeon stream (near E) 52 μm long, 31 μm wide (length to width ratio about Jujeon-campsite), 35°33ʹ08ʺN, 129°27ʹ06ʺE, 18 Apr 2021, 1.68); posterior portion protrudes slightly backward, with Shin JH. All the specimens mounted on H-S slides. 3 gac on each outside of genital sclerites, lacking sgs. Four Description. Female (DB50043): Idiosoma (Fig. 2A) 271 pairs of pgs (Fig. 2B) present around GO; foremost pgs lo­ μm long, 151 μm wide, with single sharp frontal process, 22 cated far from ahead of GO; succeeding 3 pgs situated at μm long, protruding forward on anterior edge of body. AD, near anterolateral margin, middle, and posterolateral margin PD and OC separated and ornamented with numerous fove­ of GO, respectively.

Korean name: 1*거북등짠물응애 (신칭)

Anim. Syst. Evol. Divers. 37(3), 242-248 243 Jong Hak Shin, Jimin Lee, Cheon Young Chang

Gnathosoma (Fig. 2C) 84 μm long, 49 μm wide (length to of gac on posterior genital sclerites was also variable: two width ratio about 1.71). Rostrum 42 μm long, similar length pairs of gac in two specimens, three pairs in one specimen, to gnathosomal base; tip of rostrum extending to anterior while two and three gac in each side in a specimen from Po­ edge of P-2, in ventral view. Gnathosoma with 4 pairs of hang (DB50042). Genu I showed armature of a stout fang- rostral setae: proto- and deutorostral setae situated along like and a sharp spiniform setae ventrally in three females, distal and sub-distal edge, respectively; tritorostral setae while two stout fang-like setae ventrally in the female from long, naked and located at level of posterior 70% rostrum Pohang (DB50041) (Fig. 3H). The female from Gyeongsan ventrally; basirostral setae the longest, 1.45 times longer (DB50040) has a comb row of 10-15 teeth along the inner than tritorostrals one, naked, and situated at base of rostrum. surface of lateral claws, while the three specimens from the Palp consisting of 4 segments; lengths of P-1 to P-4 10, 33, other two localities showed a row of 4-7 setules near the 11, 30 μm long, respectively; P-1 the shortest, without setae; middle of ventral edges of lateral claws. One female speci­ P-2 the longest, about 3 times longer than P-1 or P-3, with men from Pohang (DB50041) showed only three pectinate 1 long dorsal seta anteriorly; P-3 subequal to length of P-1, setae without a ventral spiniform seta on the tibia of the left armed with 1 short spiniform seta on its inner-distal corner, leg II (Fig. 3I). 5 μm long; P-4 with 3 long setae subproximally, 1 short seta Distribution. Europe (Romijn and Viets, 1924; Green and inner-distally, and bifurcated distal end. Chelicera (Fig. 2D) MacQuitty, 1987; Bartsch, 2008), Africa (Walter and Bader, 83 μm long; movable digit formed a spine 14 μm long, with 1952; Bartsch, 2008, 2013, 2018), Iran (Pesic et al., 2006), several minute denticles on inner surface. Vietnam (Bartsch, 2014), Russia (Stolbov et al., 2018), Can­ Chaetotaxy of legs (tarsi excluded) (Fig. 3A-D): trochan­ ada (Bartsch, 2011), Hawaiian Islands (Imamura, 1981), ters 1-1-1-0; basifemora 3-3-2-2; telofemora 5-4-3-2; genua U.S.A. (Bartsch, 2011), Korea. 6-6-3-3; tibiae 8-7-5-6. Genu I with 4 filiform setae dorsally, Remarks. In the genus Lobohalacarus Viets, 1939, eight 1 stout fang-like and 1 sharp spiniform setae ventrally. Tibia species or subspecies are currently recorded (FADA, 2021). I with 4 filiform setae dorsally, 2 sharp spiniform and 2 stout Among them, L. processifer (Walter, 1919) from Peru and L. fang-like setae ventrally. Tibiae II-IV with 2, 1, 2 pectinate bucharensis Jankovskaja, 1967 from Kizylkum Desert, Uz­ setae (Fig. 3B-D) on ventral surface, respectively. Tarsus I bekistan should be regarded as species inquirenda, because (Fig. 3A, E) with 3 filiform setae dorsally, 1 solenidion, 2 they were obviously based on protonymphs and/or deu­ filiform setae ventrally, 2 doublets pas on both laterally, and tonymphs (Bartsch, 2008). 1 stout fang-like seta ventrolaterally; lateral membrane of Lobohalacarus hummelincki Viets, 1940 from Venezuela claw fossa swollen. Tarsus II (Fig. 3B, F) with 3 filiform se­ and L. bunurong Harvey, 1988 from Australia are similar to tae dorsally, 1 solenidion, 1 filiform seta ventrally, a pair of L. weberi (Bartsch, 2008, 2018) in sharing 2, 1, 2 pectinate pas. Tarsus III (Fig. 3C) with 4 dorsal and 1 ventral filiform setae on the ventral surface of tibiae II to IV, respectively. setae, and a pair of pointed pas. Tarsus IV (Fig. 3D) with However, L. hummelincki differs from L. weberi by two 3 dorsal and 1 ventral filiform setae, and a pair of point­ pairs of pgs, one to two gac each side of GO, and tarsus IV ed pas. Solenidion on tarsi I and II approximately 2/3 and without ventral seta (Viets, 1940), and L. bunurong is dis­ 1/2 as long as adjacent dorsal seta, respectively (Fig. 3E, criminated from L. weberi by a pair of pgs and P-4 with two F). Lateral claws on tarsus I slightly smaller than those on basal setae (Harvey, 1988). Lobohalacarus subterraneus succeeding tarsi, smooth ventrally, with 2-3 tiny accessory Bartsch, 1995 from New Zealand is clearly distinguished processes dorsally. Lateral claws on tarsi II-IV with 2-3 ac­ from L. weberi by three pairs of sgs, two ventral spiniform cessory processes dorsally and a row of about 4-7 spinules setae (lacking a stout fang-like seta ventrally) in genu I, only along ventral edges. Median claws on tarsi I-IV present and a pectinate seta on tibia III throughout all legs, and no ven­ armed with 1 tooth dorsally. tral setae in tarsi III and IV (Bartsch, 1995b). Male: Not collected. Two subspecies of L. weberi are recognized as valid: L. Measurements and variability. Four adult female spec­ weberi gotoensis Imamura, 1970 and L. weberi tristanensis imens were examined and measured: idiosomal lengths Bartsch, 1995. Lobohalacarus weberi gotoensis Imamura, ranged from 261 to 328 μm (mean 291 μm, standard devi­ 1970 from Japan differs from L. weberi weberi by five pairs ation 30.76), idiosomal widths ranged from 166 to 203 μm of ds, including single pair of ds each on AD and OC (while (mean 178 μm, standard deviation 23.57), and mean ratio seven pairs containing two on AD and OC, respectively, in L. of length to width 1.64. The number of pgs around GO was weberi weberi) and by a single plumose seta on tibia III only slightly variable: four pairs of pgs in two specimens, five (while 2, 1, 2 pectinate setae on tibiae II-IV in L. weberi pairs in one specimen, while three and four pgs in each side weberi) (Imamura, 1970). The other subspecies, L. weberi in the specimen from Gyeongsan (DB50040). The number tristanensis Bartsch, 1995 from Tristan da Cunha Islands in

244 Anim. Syst. Evol. Divers. 37(3), 242-248 Lobohalacarus weberi (Halacaridae), New Record from Korea

A B

E

C D

Fig. 2. Lobohalacarus weberi, female (DB50043). A, Idiosoma, dorsal; B, Idiosoma, ventral; C, Gnathosoma, ventral; D, Chelicera, dorsal; E, Genital opening, ventral. Scale bars: A, B=100 μm, C-E=50 μm.

Anim. Syst. Evol. Divers. 37(3), 242-248 245 Jong Hak Shin, Jimin Lee, Cheon Young Chang

A D

B

G

H

I F

E

C

Fig. 3. Lobohalacarus weberi, female. A-F (DB50043): A-D, Legs I-IV, ventromedial; E, Tarsus I, lateral; F, Tarsus II, medial. G (DB50040), Tarsus IV, medial. H, I (DB50041): H, Variation of genu I with two stout fang-like setae, ventral; I, Variation of tibia II with three pectinate setae, ventral. Scale bars: A-D, H =50 μm, E-G, I=20 μm.

246 Anim. Syst. Evol. Divers. 37(3), 242-248 Lobohalacarus weberi (Halacaridae), New Record from Korea the South Atlantic is distinguished from L. weberi weberi by (Arach. Acari: Halacaridae). Verhandlungen des Naturwis­ the anterior idiosoma forming arch-like with a small round senschaftlichen Vereins in Hamburg, 24:5-18. edge or with a spine-like process (while always with a fron­ Bartsch I, 1995a. A new subspecies of the freshwater halacarid tal spine-like process in L. weberi weberi) and no ventral se­ mite Lobohalacarus weberi (Romijn and Viets) (Halacari­ tae on the telofemur III and tarsus IV (while one ventral seta dae, Acari) from a southern Atlantic Ocean Island. Annals of the Cape Provincial Museums, Natural History, 19:171- each on those regions in L. weberi weberi) (Bartsch, 1995a). 180. Korean specimens are well accorded with the typical ar­ Bartsch I, 1995b. Lobohalacarus subterraneus n. sp., a fresh­ mature of L. weberi, that is, a frontal spine-like process, the water halacarid (Acari: Halacaridae) from New Zealand. arrangement of both dorsal and ventral plates and dorsal New Zealand Journal of Zoology, 22:209-212. https://doi.or setae, ornamentation of pgs in GA area and gac in genital g/10.1080/03014223.1995.9518035 sclerites, and the chaetotaxy of legs, including tibiae II to Bartsch I, 2006. 5. Acari: Halacaroidea. In: Süßwasserfauna IV with 2, 1, 2 pectinate setae, respectively. However, the von Mitteleuropa 7/2-1, : Araneae, Acari I (Ed., Korean specimens show some minor individual variabilities Gerecke R). Elsevier, Spektrum, Heidelberg, pp. 113-157. in the number of pgs and gac, the setal armature on genua of Bartsch I, 2008. Freshwater halacarid mites (Halacaridae: legs, and the shape of spinule row on lateral claws, as men­ Prostigmata: Acari) from Tunesia, three new records and tioned above in the “Measurements and variability”. notes on geographical distribution of these species. Ento­ The male of L. weberi is extremely rare or could be com­ mologische Mitteilungen aus dem Zoologischen Museum pletely absent (Bartsch, 1981). In Korea, only females Hamburg, 15:15-27. Bartsch I, 2011. North American freshwater Halacaridae were found. Another semi-subterranean halacarid species, (Acari): literature survey and new records. International Soldanellonyx monardi Walter, 1919 co-occurred with this Journal of Acarology, 37:490-510. https://doi.org/10.1080/0 species in a hillside well at Gyeongsan. 1647954.2010.525528 Bartsch I, 2013. Freshwater halacarid mites (Acari: Halaca­ ridae) from Madagascar. New records and the descrip­ ORCID tion of a new species. Acarologia, 53:77-87. https://doi. org/10.1051/acarologia/20132080

Jong Hak Shin: https://orcid.org/0000-0002-1889-4212 Bartsch I, 2014. New records of freshwater Halacaridae (Acari) Jimin Lee: https://orcid.org/0000-0001-9004-8275 from the oriental region and a supplementary description of Soldanellonyx visurgis. Internaltional Journal of Acarology, Cheon Young Chang: http://orcid.org/0000-0001-5557-7120 40:165-173. https://doi.org/10.1080/01647954.2014.89736 9 Bartsch I, 2018. Freshwater halacarid (Acari: Halacaridae) from CONFLICTS OF INTEREST Madagascar: new records, keys and notes on distribution and biology. Bonn Zoological Bulletin, 67:79-99. No potential conflict of interest relevant to this article was FADA, 2021. Lobohalacarus Viets, 1939 [Internet]. Accessed reported. 4 Jun 2021, . Green J, MacQuitty M, 1987. Halacarid mites. Synopses of the ACKNOWLEDGMENTS British Fauna, New Series, 36:1-178. Harvey MS, 1988. A new species of Lobohalacarus from Aus­ tralia (Chelicerata: Acarina: Halacaridae). Memoirs of the We are grateful to two anonymous reviewers for their crit­ Museum of Victoria, 49:363-365. https://doi.org/10.24199/ ical comments that greatly improved the manuscript. This j.mmv.1988.49.15 work was supported in part by the research grant of Daegu Imamura T, 1968. Results of the speleological survey in South University, Korea in 2020 to Cheon Young Chang. Korea 1966. IX. Halacaridae (Acari) found in a limestone cave of South Korea. Bulletin of the National Science Mu­ seum, Tokyo, 11:281-284. REFERENCES Imamura T, 1970. The fauna of the insular lava caves in West Japan. II. Porohalacaridae (Acari). Bulletin of the National Bartsch I, 1975. Zur Kenntnis der Halacaridenfauna (Acari) Science Museum, Tokyo, 13:455-458. der Quellenregion, I. Ein Beitrag zur Morphologie und Bi­ Imamura T, 1981. Fresh-water halacarid mites from Oahu Is­ ologie dreier Arten aus dem Sphagnetum. Gewässer und land, Hawaii. Annotationes Zoological Japonenses, 54:287- Abwässer, 57/58:27-42. 292. Bartsch I, 1981. Meeresmilben der Umgebung von Hamburg Lee J, Chang CY, 2017. Scaptognathus teuriensis, a new record

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